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The Stability and Release profile of Some Drugs in Dika Fat Supposition Base

By Megwa, Stella Anagam

A solid vegetable fat derived from the seeds of Irvingia gabonensis was investigated either in its pure form or in combination with Olive oil and nonionic surfactants as suppository base. the results obtained are compared with those obtained using the conventional cocoa butter base.

Published: 02/12/2018

Tags: drugs, release profile, stability, Dika Fat Suppositon Base, pharmaceutical

Size: 600.48KB

Scope and Practice of Clinical Pharmacy

By Aguwa, C. N.

Seminar Paper

Published: 12/12/1993

Size: 2.03MB

Evaluation of the Antimicrobial Activities of the Volatile Oil of the Seeds of Monodora Myristica Graeth and Monodora Tenuifolia Benth (Family: Annonaceae)

By Ezejiofor, Maduabuchi

The antimicrobial activities of the volatile oil of the seeds of Monodora myristica Gaerth and Monodora tenuifolia Benth (Family Annonaceae) was evaluated using the volatile oil of the flower bud of clove, Syzygium aromaticum as standard, also known antibacterial and anti-fungal drugs were used like Trimethoprim and Sulphamethoxazole (Septrin) and ketoconazole (Nizoral).

Published: 20/01/2003

Tags: antimicrobial, volatile oil, seeds, mondora myristica graeth, monodora tenuifolia

Size: 20.54MB

Study on Waxy Matrix Drug Delivery Systems Containing Cellulose produced Using Trona as an Artificial Chaperon

By Akpa, Chile, Paul

The potential uses of pharmaceutical grade cellulose in the pharmaceuticaI
industry is the raison d itre for this work. Cellulose was extracted from sawdust
obtained from the tropical tree Gmelinu ai.borea Family Verbenaceae by means of
the classical soda process.
The pure a -cellulose produced was then treated with various concentrations
of trona (sodium sesquicarbonate) 0. I%, I%, 2%, 5%, 15%, and 20% . The trona
treated cellulose named "tronated microfine cellulose "(TMFC) along with
untronated a-cellulose was subsequently subjected to physico-chemical
evaluation. Properties evaluated included microscopical characteristics ,densification
behaviour ,elemental analysis, simple sugar composition, and swelling characteristics
among others.
Next, the cellulose powders were then investigated to ascertain their
compatibility with two model drugs namely acetaminophen and ascorbic acid by
means of the temperature stress technique. The celluloses were then employed as
channelling agents in waxy matrix drug delivery systems .These extrusion matrices
were produced using a locally designed and fabricated matrix making unit(MMU).
The matrix forming materials used were dika fat and paraffin wax. Physical
properties of representative samples of the matrices such as weight, dimensions and
friability were determined . Drug release studies were then conducted in 0.1 HCL.
Results of the physicochemical studies revealed that TMFC has the typical
MFC microscopic morphology, bulk volume of between 3.02-5.10cm3 ,bulk density
of 0.28-0.57gl cm3 ,Hausner9s ratio of 1.20-1 .SO and percentage compressibility
of between 34-42 %. The drug compatibility studies revealed no degradation
products. The matrices weighed 400mg on the average, had dimensions of 12mm by
3mm and had friability of O.OS%.The results of the drug release studies indicated that
release followed a diffusion controlled matrix mode!, where the quantity of drug
released is proportional to the square root of time. Further analysis of the release data
revealed that release rate tended to increase with increasing amounts of the
channelling agent. A 15-50% quantity of acetaminophen was released in the first
hour of study with matrices containing higher proportions of channelling agent
having correspondingly higher rates of release. A similar behaviour was observed
with the matrices containing ascorbic acid though at Iower concentration levels.
The results obtained in this study convincingly indicate that cellulose can be
extracted from sawdust, the cellulose so produced can be transformed into a grade of
MFC using trona as an artificial chaperon. It was also found that TMFC can be
successfully employed as a channelling agent in waxy matrix drug delivery system
(WDDS) for oral sustained release formulations.

Published: 23/01/2001

Size: 14.59MB